Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene.

Polymorphic DNA markers can now be used for presymptomatic and prenatal diagnosis of the autosomal dominant form of polycystic kidney disease (PKD). A detailed map is known for the chromosomal region around the PKD1 gene on the short arm of chromosome 16. We present here a simple, two step procedure...

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Autors principals: Breuning, M H, Snijdewint, F G, Dauwerse, J G, Saris, J J, Bakker, E, Pearson, P L, vanOmmen, G J
Format: Artigo
Idioma:Inglês
Publicat: 1990
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1017239/
https://ncbi.nlm.nih.gov/pubmed/1978861
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